Product Name

  • Name

    Diphenyl N-cyanocarbonimidate

  • EINECS 427-300-8
  • CAS No. 79463-77-7
  • Article Data2
  • CAS DataBase
  • Density 1.1 g/cm3
  • Solubility Insoluble in water.
  • Melting Point 155-158 °C(lit.)
  • Formula C14H10N2O2
  • Boiling Point 341.3 °C at 760 mmHg
  • Molecular Weight 238.246
  • Flash Point 160.2 °C
  • Transport Information
  • Appearance white fluffy powder
  • Safety S26;S36/37
  • Risk Codes R20/21/22;R36/37/38
  • Molecular Structure Molecular Structure of 79463-77-7 (Diphenyl N-cyanocarbonimidate)
  • Hazard Symbols HarmfulXn
  • Synonyms Carbonimidicacid, cyano-, diphenyl ester (9CI);Diphenoxymethylenecyanamide;DiphenylN-cyanocarbonimidate;Diphenyl N-cyanoimidocarbonate;Diphenylcyanocarbonimidate;
  • PSA 54.61000
  • LogP 2.98148

Synthetic route

CYANAMID
420-04-2

CYANAMID

dichlorodiphenoxymethane
4885-03-4

dichlorodiphenoxymethane

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

Conditions
ConditionsYield
In ethyl acetate 1.) not above 80 deg C, 2.) R.T., 3.5 h.;91%
In ethyl acetate <60 deg C;51%
bis(phenyl) carbonate
102-09-0

bis(phenyl) carbonate

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 78 percent / PCl5 / 16 h / 155 °C
2: 51 percent / ethyl acetate / <60 deg C
View Scheme
Multi-step reaction with 2 steps
1: 96 percent / phosphorus pentachloride / 1.) 160 deg C, 24 h, 2.) 200 deg 15 min.
2: 91 percent / ethyl acetate / 1.) not above 80 deg C, 2.) R.T., 3.5 h.
View Scheme
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

3-Amino-5-phenoxy-1H-1,2,4-triazole
146335-71-9

3-Amino-5-phenoxy-1H-1,2,4-triazole

Conditions
ConditionsYield
With hydrazine In methanol at 0 - 20℃; for 2h;100%
With hydrazine In isopropyl alcohol for 3h; Heating;59.5%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

aniline
62-53-3

aniline

N-cyano-N'-phenylcarbamimidic acid phenyl ester
84859-47-2

N-cyano-N'-phenylcarbamimidic acid phenyl ester

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 20℃; for 3h;100%
In isopropyl alcohol for 2h; Ambient temperature;98%
In acetonitrile at 20℃; for 18h;
In isopropyl alcohol
In isopropyl alcohol at 20℃;
N,N-dimethylammonium chloride
506-59-2

N,N-dimethylammonium chloride

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

O-phenyl-N-cyano-N',N'-dimethylurea
167494-04-4

O-phenyl-N-cyano-N',N'-dimethylurea

Conditions
ConditionsYield
In tetrahydrofuran100%
N-[(10R,14S)-5-amino-10-methyl-9-oxo-8,16-diazatricyclo[13.3.1.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-14-yl]-1-(3-chloro-2-fluorophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide dihydrochloride

N-[(10R,14S)-5-amino-10-methyl-9-oxo-8,16-diazatricyclo[13.3.1.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-14-yl]-1-(3-chloro-2-fluorophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide dihydrochloride

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

1-(3-chloro-2-fluorophenyl)-N-[(10R,14S)-5-{[(1Z)-(cyanoimino)(phenoxy)methyl]amino}-10-methyl-9-oxo-8,16-diazatricyclo[13.3.1.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-14-yl]-5-methyl-1H-1,2,3-triazole-4-carboxamide
1422448-80-3

1-(3-chloro-2-fluorophenyl)-N-[(10R,14S)-5-{[(1Z)-(cyanoimino)(phenoxy)methyl]amino}-10-methyl-9-oxo-8,16-diazatricyclo[13.3.1.02,7]nonadeca-1(19),2(7),3,5,15,17-hexaen-14-yl]-5-methyl-1H-1,2,3-triazole-4-carboxamide

Conditions
ConditionsYield
With pyridine In isopropyl alcohol at 20℃; for 2h;99%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

(R)-N-[1-(3-bromophenyl)ethyl] acetamide
176707-77-0

(R)-N-[1-(3-bromophenyl)ethyl] acetamide

(R)-N3-(1-(3-bromophenyl)ethyl)-4H-1,2,4-triazole-3,5-diamine

(R)-N3-(1-(3-bromophenyl)ethyl)-4H-1,2,4-triazole-3,5-diamine

Conditions
ConditionsYield
Stage #1: N-cyanodiphenylcarbonimidate; (R)-N-[1-(3-bromophenyl)ethyl] acetamide In isopropyl alcohol at 20 - 60℃;
Stage #2: With hydrazine hydrate In methanol at 50℃; for 4h;		99%
4-benzyloxyaniline hydrochloride
51388-20-6

4-benzyloxyaniline hydrochloride

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

C21H17N3O2
929267-13-0

C21H17N3O2

Conditions
ConditionsYield
Stage #1: 4-benzyloxyaniline hydrochloride With triethylamine In isopropyl alcohol at 20℃; for 0.166667h;
Stage #2: N-cyanodiphenylcarbonimidate In isopropyl alcohol at 20℃; for 3.5h;		98%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

4-(piperazin-1-yl)pyridine
1008-91-9

4-(piperazin-1-yl)pyridine

C17H17N5O
1400691-99-7

C17H17N5O

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;98%
(8S)-N-methyl-N-({1-[(3S)-3-piperidinylmethyl]-1H-benzimidazol-2-yl}methyl)-5,6,7,8-tetrahydro-8-quinolinamine
876590-12-4

(8S)-N-methyl-N-({1-[(3S)-3-piperidinylmethyl]-1H-benzimidazol-2-yl}methyl)-5,6,7,8-tetrahydro-8-quinolinamine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

phenyl (3R)-N-cyano-3-{[2-({methyl[(8S)-5,6,7,8-tetrahydro-8-quinolinyl]amino}methyl)-1H-benzimidazol-1-yl]methyl}-1-piperidinecarboximidoate

phenyl (3R)-N-cyano-3-{[2-({methyl[(8S)-5,6,7,8-tetrahydro-8-quinolinyl]amino}methyl)-1H-benzimidazol-1-yl]methyl}-1-piperidinecarboximidoate

Conditions
ConditionsYield
In isopropyl alcohol at 20℃;97%
3-[4-(aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4h)-one trifluoroacetate
943598-71-8

3-[4-(aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4h)-one trifluoroacetate

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

trifluoroacetic acid
76-05-1

trifluoroacetic acid

N-(3-chloro-4-fluorophenyl)-4-[((E/Z)-((cyanoimino)[(4-methoxybenzyl)amino]methyl)-amino)methyl]-N'-hydroxy-1,2,5-oxadiazole-3-carboximidamide trifluoroacetate

N-(3-chloro-4-fluorophenyl)-4-[((E/Z)-((cyanoimino)[(4-methoxybenzyl)amino]methyl)-amino)methyl]-N'-hydroxy-1,2,5-oxadiazole-3-carboximidamide trifluoroacetate

Conditions
ConditionsYield
Stage #1: 3-[4-(aminomethyl)-1,2,5-oxadiazol-3-yl]-4-(3-chloro-4-fluorophenyl)-1,2,4-oxadiazol-5(4h)-one trifluoroacetate; N-cyanodiphenylcarbonimidate With triethylamine In tetrahydrofuran at 20℃; for 2h;
Stage #2: With sodium hydroxide; water In tetrahydrofuran at 20℃; for 0.5h;
Stage #3: trifluoroacetic acid With acetic acid more than 3 stages;		97%
...Expand
(+/-)-cis-[3-(1H-imidazol-4-yl)cyclopentyl]methanamine

(+/-)-cis-[3-(1H-imidazol-4-yl)cyclopentyl]methanamine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

(+/-)-1-cyano-3-{[cis-3-(1H-imidazol-4-yl)cyclopentyl]methyl}-2-phenylisourea

(+/-)-1-cyano-3-{[cis-3-(1H-imidazol-4-yl)cyclopentyl]methyl}-2-phenylisourea

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 1h;97%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

2-(4,5-Diphenyl-1H-imidazol-2-yl)-ethylamine
88883-83-4

2-(4,5-Diphenyl-1H-imidazol-2-yl)-ethylamine

<<2-(4,5-Diphenyl-1H-imidazol-2-yl)ethylamino>phenoxymethylen>cyanamid
92095-56-2

<<2-(4,5-Diphenyl-1H-imidazol-2-yl)ethylamino>phenoxymethylen>cyanamid

Conditions
ConditionsYield
In ethanol; dichloromethane for 0.5h; Ambient temperature;96%
(3R,3AS,6AR)-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-[4-(2-aminoethoxy)benzyl]-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxypropylcarbamate
313680-01-2

(3R,3AS,6AR)-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-1-[4-(2-aminoethoxy)benzyl]-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-2-hydroxypropylcarbamate

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

(3R,3aS,6aR).-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-1-[4-(2-{[(E and/or Z)-(cyanoimino)(phenoxy)methyl]amino}ethoxy)benzyl]-2-hydroxypropylcarbamate

(3R,3aS,6aR).-hexahydrofuro[2,3-b]furan-3-yl (1S,2R)-3-[(1,3-benzodioxol-5-ylsulfonyl)(isobutyl)amino]-1-[4-(2-{[(E and/or Z)-(cyanoimino)(phenoxy)methyl]amino}ethoxy)benzyl]-2-hydroxypropylcarbamate

Conditions
ConditionsYield
With triethylamine In dichloromethane; isopropyl alcohol at 20℃; for 2.5h;96%
1-(4-methoxyphenyl)piperazine
38212-30-5

1-(4-methoxyphenyl)piperazine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

C19H20N4O2
1400691-98-6

C19H20N4O2

Conditions
ConditionsYield
In dichloromethane at 20℃; for 24h;96%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

1-(pyridin-4-ylmethyl)piperazine
62089-74-1

1-(pyridin-4-ylmethyl)piperazine

C18H19N5O
1400692-03-6

C18H19N5O

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h;96%
C14H19ClN2O

C14H19ClN2O

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

phenyl‐N‐(1‐(3‐(2‐chlorophenyl)propanoyl)piperidin‐4‐yl)‐N’‐cyanocarbamimidate

phenyl‐N‐(1‐(3‐(2‐chlorophenyl)propanoyl)piperidin‐4‐yl)‐N’‐cyanocarbamimidate

Conditions
ConditionsYield
In dichloromethane for 1h;96%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

4-(4-Aminobenzoyl)-1,3-dihydro-5-methyl-3H-imidazol-2-one
173375-23-0

4-(4-Aminobenzoyl)-1,3-dihydro-5-methyl-3H-imidazol-2-one

N1-Cyano-N2-<4-<(1,3-dihydro-5-methyl-2-oxo-3H-imidazol-4-yl)carbonyl>phenyl>-O-phenyl isourea
173375-92-3

N1-Cyano-N2-<4-<(1,3-dihydro-5-methyl-2-oxo-3H-imidazol-4-yl)carbonyl>phenyl>-O-phenyl isourea

Conditions
ConditionsYield
With pyridine for 5h; Ambient temperature;95%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

1-(3-{N'-[4-(2-Amino-ethylsulfanylmethyl)-thiazol-2-yl]-guanidinomethyl}-phenyl)-3-((R)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-urea; hydrochloride

1-(3-{N'-[4-(2-Amino-ethylsulfanylmethyl)-thiazol-2-yl]-guanidinomethyl}-phenyl)-3-((R)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-urea; hydrochloride

C33H31N11O2S2

C33H31N11O2S2

Conditions
ConditionsYield
With triethylamine In methanol for 4h; Ambient temperature;95%
N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester
70406-92-7

N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetate
146374-56-3

ethyl (2-cyanoimino-5,6-dichloro-1,2,3,4-tetrahydroquinazolin-3-yl)-acetate

Conditions
ConditionsYield
In acetonitrile for 3h; Heating;95%
In water; ethyl acetate; acetonitrile
In N-methyl-acetamide; benzene
4-morpholino-4-yl-phenylamine
2524-67-6

4-morpholino-4-yl-phenylamine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

N-cyano-N'-(4-morpholino-phenyl)-O-phenylisourea
700804-71-3

N-cyano-N'-(4-morpholino-phenyl)-O-phenylisourea

Conditions
ConditionsYield
In isopropyl alcohol for 22h;95%
In isopropyl alcohol at 100℃;
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

2,4-Dimethoxyaniline
2735-04-8

2,4-Dimethoxyaniline

N-cyano-N'-(2,4-dimethoxy-phenyl)-O-phenylisourea
700804-95-1

N-cyano-N'-(2,4-dimethoxy-phenyl)-O-phenylisourea

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 24 - 48h;95%
3-Phenylpropan-1-amine
2038-57-5

3-Phenylpropan-1-amine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

1-cyano-2-phenyl-3-(3-phenylpropyl)isourea
1192559-65-1

1-cyano-2-phenyl-3-(3-phenylpropyl)isourea

Conditions
ConditionsYield
In dichloromethane at 20℃; for 2h; Inert atmosphere;95%
In dichloromethane at 20℃; for 1h;86%
In isopropyl alcohol at 20℃; for 1h;84%
With isopropyl alcohol at 20℃; for 1h;
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

3-methoxy-4-(1,3-oxazol-5-yl)aniline
198821-79-3

3-methoxy-4-(1,3-oxazol-5-yl)aniline

C18H14N4O3
267647-77-8

C18H14N4O3

Conditions
ConditionsYield
In acetonitrile at 20℃;94%
endo 2-methyl-1-{8-[2-(4-phenylpiperidin-4-yl)ethyl]-8-azabicyclo[3.2.1]oct-3-yl}-1H-benzimidazole dihydrochloride

endo 2-methyl-1-{8-[2-(4-phenylpiperidin-4-yl)ethyl]-8-azabicyclo[3.2.1]oct-3-yl}-1H-benzimidazole dihydrochloride

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

phenyl N-cyano-4-{2-[3-(2-methyl-1H-benzimidazol-1-yl)-8-azabicyclo[3.2.1]oct-8-yl]ethyl}-4-phenylpiperidine-1-carboximidoate

phenyl N-cyano-4-{2-[3-(2-methyl-1H-benzimidazol-1-yl)-8-azabicyclo[3.2.1]oct-8-yl]ethyl}-4-phenylpiperidine-1-carboximidoate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 4h;94%
methyl 4-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)sulfonyl]methylpiperidine-4-carboxylate
869189-73-1

methyl 4-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)sulfonyl]methylpiperidine-4-carboxylate

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

methyl 1-[(cyanoimino)(phenoxy)methyl]-4-{[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)sulfonyl]methyl}piperidine-4-carboxylate

methyl 1-[(cyanoimino)(phenoxy)methyl]-4-{[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)sulfonyl]methyl}piperidine-4-carboxylate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at 90℃; for 16h;94%
endo 2-methyl-1-{8-[2-(4-phenylpiperidin-4-yl)ethyI]-8-azabicyclo[3.2.1]oct-3-yl}-1H-benzimidazole
716348-30-0

endo 2-methyl-1-{8-[2-(4-phenylpiperidin-4-yl)ethyI]-8-azabicyclo[3.2.1]oct-3-yl}-1H-benzimidazole

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

phenyl N-cyano-4-{2-[3-(2-methyl-1H-benzimidazol-1-yl)-8-azabicyclo[3.2.1]oct-8-yl]ethyl}-4-phenylpiperidine-1-carboximidoate

phenyl N-cyano-4-{2-[3-(2-methyl-1H-benzimidazol-1-yl)-8-azabicyclo[3.2.1]oct-8-yl]ethyl}-4-phenylpiperidine-1-carboximidoate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 4h;94%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

2-phenoxyethanamine
1758-46-9

2-phenoxyethanamine

1-cyano-2-phenyl-3-[2-(phenoxy)ethyl]isourea

1-cyano-2-phenyl-3-[2-(phenoxy)ethyl]isourea

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 1h;94%
3-Aminomethylpyridine
3731-52-0

3-Aminomethylpyridine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

phenyl N'-cyano-N-(pyridin-3-ylmethyl)carbamimidate

phenyl N'-cyano-N-(pyridin-3-ylmethyl)carbamimidate

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 18h;94%
3-(3-aminopropoxy)-N,N-dimethylbenzenemethanamine
69384-05-0

3-(3-aminopropoxy)-N,N-dimethylbenzenemethanamine

N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

N'-cyano-N-<3-<3-<(dimethylamino)methyl>phenoxy>propyl>-O-phenylisourea
84035-82-5

N'-cyano-N-<3-<3-<(dimethylamino)methyl>phenoxy>propyl>-O-phenylisourea

Conditions
ConditionsYield
In diethyl ether for 1h; Ambient temperature;92%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

2-benzimidazolylcarbamonitrile
55864-37-4

2-benzimidazolylcarbamonitrile

Conditions
ConditionsYield
In isopropyl alcohol for 1h; Heating;92%
N-cyanodiphenylcarbonimidate
79463-77-7

N-cyanodiphenylcarbonimidate

4-{[(2-aminoethyl)thio]methyl}-5-methylimidazole
38585-67-0

4-{[(2-aminoethyl)thio]methyl}-5-methylimidazole

N-<2<<(5-methyl-1H-imidazol-4-yl)methyl>thio>ethyl>-N'-cyano-O-phenylisourea
110821-25-5, 112528-18-4, 112528-19-5

N-<2<<(5-methyl-1H-imidazol-4-yl)methyl>thio>ethyl>-N'-cyano-O-phenylisourea

Conditions
ConditionsYield
With potassium carbonate In water; ethyl acetate for 4h;92%
In diethyl ether for 1h; Ambient temperature; Yield given;

Diphenyl N-cyanocarbonimidate Chemical Properties

Molecular Structure of Diphenyl N-cyanocarbonimidate (CAS NO.79463-77-7):

IUPAC Name: diphenoxymethylidenecyanamide 
Empirical Formula: C14H10N2O2
Molecular Weight: 238.2414
H bond acceptors: 4
H bond donors: 0
Freely Rotating Bonds: 4
Polar Surface Area: 54.61 Å2
Index of Refraction: 1.56
Molar Refractivity: 69.71 cm3
Molar Volume: 215.4 cm3
Surface Tension: 42.6 dyne/cm
Density: 1.1 g/cm3
Flash Point: 160.2 °C
Enthalpy of Vaporization: 58.49 kJ/mol
Boiling Point: 341.3 °C at 760 mmHg
\Vapour Pressure: 8.13E-05 mmHg at 25°C
EINECS: 427-300-8
Product Categories: Aromatic Nitriles; Amidates/Imidates; Nitrogen Compounds; Organic Building Blocks
SMILES: N#C\N=C(/Oc1ccccc1)Oc2ccccc2
InChI: InChI=1/C14H10N2O2/c15-11-16-14(17-12-7-3-1-4-8-12)18-13-9-5-2-6-10-13/h1-10H

Diphenyl N-cyanocarbonimidate Safety Profile

Hazard Codes: HarmfulXn
Risk Statements: 20/21/22-36/37/38
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed. 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36/37
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36/37:Wear suitable protective clothing and gloves.
RIDADR: 3439
WGK Germany: 3
F: 10-21
HazardClass: 6.1
PackingGroup: III

Diphenyl N-cyanocarbonimidate Specification

  Diphenyl N-cyanocarbonimidate , with CAS number of 79463-77-7, can be called Carbonimidic acid, cyano-, diphenyl ester ; carbonimidic acid, N-cyano-, diphenyl ester . It is a white fluffy powder.

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